Radiotherapy & Oncology
Volume 101, Issue 2 , Pages 329-336, November 2011

Soy isoflavones radiosensitize lung cancer while mitigating normal tissue injury

  • Gilda G. Hillman

      Affiliations

    • Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, USA
    • Corresponding Author InformationCorresponding author. Address: Department of Radiation Oncology, Wayne State University School of Medicine, 515 Hudson-Webber Cancer Research Center, 4100 John R. Road, Detroit, MI 48201, USA.
  • ,
  • Vinita Singh-Gupta

      Affiliations

    • Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, USA
  • ,
  • Lindsay Runyan

      Affiliations

    • Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, USA
  • ,
  • Christopher K. Yunker

      Affiliations

    • Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, USA
  • ,
  • Joseph T. Rakowski

      Affiliations

    • Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, USA
  • ,
  • Fazlul H. Sarkar

      Affiliations

    • Department of Pathology, Wayne State University School of Medicine, Detroit, USA
  • ,
  • Steven Miller

      Affiliations

    • Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, USA
  • ,
  • Shirish M. Gadgeel

      Affiliations

    • Internal Medicine, Wayne State University School of Medicine, Detroit, MI, USA
  • ,
  • Seema Sethi

      Affiliations

    • Department of Pathology, Wayne State University School of Medicine, Detroit, USA
  • ,
  • Michael C. Joiner

      Affiliations

    • Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, USA
  • ,
  • Andre A. Konski

      Affiliations

    • Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, USA

Received 18 July 2011; received in revised form 27 October 2011; accepted 30 October 2011. published online 14 November 2011.

Abstract 

Background

We have demonstrated that soy isoflavones radiosensitize cancer cells. Prostate cancer patients receiving radiotherapy (RT) and soy tablets had reduced radiation toxicity to surrounding organs. We have now investigated the combination of soy with RT in lung cancer (NSCLC), for which RT is limited by radiation-induced pneumonitis.

Methods

Human A549 NSCLC cells were injected i.v. in nude mice to generate lung tumor nodules. Lung tumor-bearing mice were treated with left lung RT at 12Gy and with oral soy treatments at 1mg/day for 30days. Lung tissues were processed for histology.

Results

Compared to lung tumor nodules treated with soy isoflavones or radiation, lung tissues from mice treated with both modalities showed that soy isoflavones augmented radiation-induced destruction of A549 lung tumor nodules leading to small residual tumor nodules containing degenerating tumor cells with large vacuoles. Soy isoflavones decreased the hemorrhages, inflammation and fibrosis caused by radiation in lung tissue, suggesting protection of normal lung tissue.

Conclusions

Soy isoflavones augment destruction of A549 lung tumor nodules by radiation, and also mitigate vascular damage, inflammation and fibrosis caused by radiation injury to normal lung tissue. Soy could be used as a non-toxic complementary approach to improve RT in NSCLC.

Keywords: Lung cancer, Soy isoflavones, Radiation

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0167-8140(11)00636-0

doi:10.1016/j.radonc.2011.10.020

Radiotherapy & Oncology
Volume 101, Issue 2 , Pages 329-336, November 2011